Similar articles for PMID: 12112109

Year	Number of Results
1999	1
2000	10
2001	20
2002	12
2003	16
2004	7
2005	7
2006	4
2007	4
2008	4
2009	9
2010	7
2011	1
2012	4
2013	2
2014	3
2015	2
2016	4
2017	4
2018	5
2019	1
2020	3
2021	2
2024	0

1

Role of parkin mutations in 111 community-based patients with early-onset parkinsonism.

Kann M, Jacobs H, Mohrmann K, Schumacher K, Hedrich K, Garrels J, Wiegers K, Schwinger E, Pramstaller PP, Breakefield XO, Ozelius LJ, Vieregge P, Klein C. Kann M, et al. Ann Neurol. 2002 May;51(5):621-5. doi: 10.1002/ana.10179. Ann Neurol. 2002. PMID: 12112109

2

Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations.

Lücking CB, Bonifati V, Periquet M, Vanacore N, Brice A, Meco G. Lücking CB, et al. Neurology. 2001 Sep 11;57(5):924-7. doi: 10.1212/wnl.57.5.924. Neurology. 2001. PMID: 11552035

3

Parkin mutations are frequent in patients with isolated early-onset parkinsonism.

Periquet M, Latouche M, Lohmann E, Rawal N, De Michele G, Ricard S, Teive H, Fraix V, Vidailhet M, Nicholl D, Barone P, Wood NW, Raskin S, Deleuze JF, Agid Y, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease. Periquet M, et al. Brain. 2003 Jun;126(Pt 6):1271-8. doi: 10.1093/brain/awg136. Brain. 2003. PMID: 12764050

4

Parkin mutation dosage and the phenomenon of anticipation: a molecular genetic study of familial parkinsonism.

Poorkaj P, Moses L, Montimurro JS, Nutt JG, Schellenberg GD, Payami H. Poorkaj P, et al. BMC Neurol. 2005 Feb 22;5(1):4. doi: 10.1186/1471-2377-5-4. BMC Neurol. 2005. PMID: 15725358 Free PMC article.

5

Homozygous partial genomic triplication of the parkin gene in early-onset parkinsonism.

Mata IF, Alvarez V, Coto E, Blazquez M, Guisasola LM, Salvador C, Kachergus JM, Lincoln SJ, Farrer M. Mata IF, et al. Neurosci Lett. 2005 Jun 3;380(3):257-9. doi: 10.1016/j.neulet.2005.01.051. Epub 2005 Feb 8. Neurosci Lett. 2005. PMID: 15862897

6

Homozygous exon 4 deletion in parkin gene in a Korean family with autosomal recessive early onset parkinsonism.

Kim JS, Lee KS, Kim YI, Lee KH, Kim HT. Kim JS, et al. Yonsei Med J. 2003 Apr 30;44(2):336-9. doi: 10.3349/ymj.2003.44.2.336. Yonsei Med J. 2003. PMID: 12728478 Free article.

7

Association between early-onset Parkinson's disease and mutations in the parkin gene.

Lücking CB, Dürr A, Bonifati V, Vaughan J, De Michele G, Gasser T, Harhangi BS, Meco G, Denèfle P, Wood NW, Agid Y, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease. Lücking CB, et al. N Engl J Med. 2000 May 25;342(21):1560-7. doi: 10.1056/NEJM200005253422103. N Engl J Med. 2000. PMID: 10824074 Free article.

8

The nigrostriatal dopaminergic system in familial early onset parkinsonism with parkin mutations.

Portman AT, Giladi N, Leenders KL, Maguire P, Veenma-van der Duin L, Swart J, Pruim J, Simon ES, Hassin-Baer S, Korczyn AD. Portman AT, et al. Neurology. 2001 Jun 26;56(12):1759-62. doi: 10.1212/wnl.56.12.1759. Neurology. 2001. PMID: 11425950

9

The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonism.

Hedrich K, Kann M, Lanthaler AJ, Dalski A, Eskelson C, Landt O, Schwinger E, Vieregge P, Lang AE, Breakefield XO, Ozelius LJ, Pramstaller PP, Klein C. Hedrich K, et al. Hum Mol Genet. 2001 Aug 1;10(16):1649-56. doi: 10.1093/hmg/10.16.1649. Hum Mol Genet. 2001. PMID: 11487568

10

Parkin mutations and early onset parkinsonism.

Morrison KE. Morrison KE. Brain. 2003 Jun;126(Pt 6):1250-1. doi: 10.1093/brain/awg189. Brain. 2003. PMID: 12764048 No abstract available.

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